Haruta M - Search Results

1

Narrowed abrogation of the Angelman syndrome critical interval on human chromosome 15 does not interfere with epigenotype maintenance in somatic cells.

Haruta M, Meguro M, Sakamoto YK, Hoshiya H, Kashiwagi A, Kaneko Y, Mitsuya K, Oshimura M. Haruta M, et al. J Hum Genet. 2005;50(3):124-132. doi: 10.1007/s10038-005-0231-2. Epub 2005 Mar 3. J Hum Genet. 2005. PMID: 15744456

2

Predominant maternal expression of the mouse Atp10c in hippocampus and olfactory bulb.

Kashiwagi A, Meguro M, Hoshiya H, Haruta M, Ishino F, Shibahara T, Oshimura M. Kashiwagi A, et al. Among authors: haruta m. J Hum Genet. 2003;48(4):194-8. doi: 10.1007/s10038-003-0009-3. Epub 2003 Mar 12. J Hum Genet. 2003. PMID: 12730723

3

A new imprinted cluster on the human chromosome 7q21-q31, identified by human-mouse monochromosomal hybrids.

Okita C, Meguro M, Hoshiya H, Haruta M, Sakamoto YK, Oshimura M. Okita C, et al. Among authors: haruta m. Genomics. 2003 Jun;81(6):556-9. doi: 10.1016/s0888-7543(03)00052-1. Genomics. 2003. PMID: 12782124

4

Association of 11q loss, trisomy 12, and possible 16q loss with loss of imprinting of insulin-like growth factor-II in Wilms tumor.

Watanabe N, Nakadate H, Haruta M, Sugawara W, Sasaki F, Tsunematsu Y, Kikuta A, Fukuzawa M, Okita H, Hata J, Soejima H, Kaneko Y. Watanabe N, et al. Among authors: haruta m. Genes Chromosomes Cancer. 2006 Jun;45(6):592-601. doi: 10.1002/gcc.20321. Genes Chromosomes Cancer. 2006. PMID: 16518847

5

Promoter hypermethylation of the RASSF1A gene predicts the poor outcome of patients with hepatoblastoma.

Sugawara W, Haruta M, Sasaki F, Watanabe N, Tsunematsu Y, Kikuta A, Kaneko Y. Sugawara W, et al. Among authors: haruta m. Pediatr Blood Cancer. 2007 Sep;49(3):240-9. doi: 10.1002/pbc.21031. Pediatr Blood Cancer. 2007. PMID: 16937357

6

Duplication of the paternal IGF2 allele in trisomy 11 and elevated expression levels of IGF2 mRNA in congenital mesoblastic nephroma of the cellular or mixed type.

Watanabe N, Haruta M, Soejima H, Fukushi D, Yokomori K, Nakadate H, Okita H, Hata JI, Fukuzawa M, Kaneko Y. Watanabe N, et al. Among authors: haruta m. Genes Chromosomes Cancer. 2007 Oct;46(10):929-35. doi: 10.1002/gcc.20481. Genes Chromosomes Cancer. 2007. PMID: 17639583

7

Combined BubR1 protein down-regulation and RASSF1A hypermethylation in Wilms tumors with diverse cytogenetic changes.

Haruta M, Matsumoto Y, Izumi H, Watanabe N, Fukuzawa M, Matsuura S, Kaneko Y. Haruta M, et al. Mol Carcinog. 2008 Sep;47(9):660-6. doi: 10.1002/mc.20412. Mol Carcinog. 2008. PMID: 18286482

8

Duplication of paternal IGF2 or loss of maternal IGF2 imprinting occurs in half of Wilms tumors with various structural WT1 abnormalities.

Haruta M, Arai Y, Sugawara W, Watanabe N, Honda S, Ohshima J, Soejima H, Nakadate H, Okita H, Hata J, Fukuzawa M, Kaneko Y. Haruta M, et al. Genes Chromosomes Cancer. 2008 Aug;47(8):712-27. doi: 10.1002/gcc.20572. Genes Chromosomes Cancer. 2008. PMID: 18464243

9

The methylation status of RASSF1A promoter predicts responsiveness to chemotherapy and eventual cure in hepatoblastoma patients.

Honda S, Haruta M, Sugawara W, Sasaki F, Ohira M, Matsunaga T, Yamaoka H, Horie H, Ohnuma N, Nakagawara A, Hiyama E, Todo S, Kaneko Y. Honda S, et al. Among authors: haruta m. Int J Cancer. 2008 Sep 1;123(5):1117-25. doi: 10.1002/ijc.23613. Int J Cancer. 2008. PMID: 18537155

10

Loss of imprinting of IGF2 correlates with hypermethylation of the H19 differentially methylated region in hepatoblastoma.

Honda S, Arai Y, Haruta M, Sasaki F, Ohira M, Yamaoka H, Horie H, Nakagawara A, Hiyama E, Todo S, Kaneko Y. Honda S, et al. Among authors: haruta m. Br J Cancer. 2008 Dec 2;99(11):1891-9. doi: 10.1038/sj.bjc.6604754. Epub 2008 Oct 28. Br J Cancer. 2008. PMID: 19034281 Free PMC article.

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